This submission belongs to the session a. General Organic Synthesis of the event The 19th International Electronic Conference on Synthetic Organic Chemistry
Published date
30 Oct, 2015
Citation
Faranak Manteghi, Reza Tondfekr, Negin Khatibi, Catalyzing Strecker Reaction by a Layered Double Hydroxide, in Proceedings of The 19th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2015, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-19-a033
Share
Email
Facebook
Twitter
LinkedIn
Catalyzing Strecker Reaction by a Layered Double Hydroxide
Reza Tondfekr 1
Faranak Manteghi 1
Negin Khatibi 1
1. Department of Chemistry, Iran University of Science and Technology, Tehran, Iran
Abstract
Layered double hydroxides (LDHs), have attracted attentions because of their layered structure and high anion-exchange capacity [1]. Positively charged brucite-like layers with interlayer spaces containing anions and water molecules form LDHs structure. Overall structure of LDHs makes it suitable as a heterogeneous catalyst for organic reactions [2-3].Strecker reaction is an important process in α-aminonitriles synthesis. α-Aminonitriles play key roles in pharmaceutical industry, especially in preparation of α-amino acid and the various nitrogen and sulfur containing heterocycles[4]. Mentioned reaction can be mediated by homogenous catalysts with high yields. Although homogenous catalysts are highly efficient, they are expensive, toxic and need tedious work up. So heterogeneous catalysts such as molecular sieves, natural polymers, nano-sized materials and metal organic frameworks are some promising alternatives for this three-component reaction [5]. In this study, we used LDH as a heterogeneous catalyst for Strecker reaction, which resulted in high yields and short reaction time.
Keywords
layered double hydroxide
Strecker reaction
transition metals
heterogeneous catalysts
Manuscript
Tondfekr main ecsoc 2015.pdf
Asymmetric synthesis of a to nitrogen substituted azaheterocycles. Application to the total synthesis of S-(-)-Anabasine.
Diastereoselectivity in the Ring Expansion of Tetrahydropyrimidin-2-ones into Tetrahydro-1H-1,3-diazepin-2-ones